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Quaderni Sclavo Di Diagnostica Clinica E Di Laboratorio|September 1, 1983
[Evaluation of the immunoenzymatic method for the study of rubella virus antibodies in relation to the traditional hemagglutination-inhibition test]P Quaglio, A Dattoli, G Aggazzotti, et al.
International Journal of Radiation Oncology, Biology, Physics|February 1, 1997
Low risk of urinary incontinence following prostate brachytherapy in patients with a prior transurethral prostate resectionK Wallner, H Lee, S Wasserman, et al.
Oncology (Williston Park, N.Y.)|August 25, 2007
Reviving the acid phosphatase test for prostate cancerAl Taira, Gregory Merrick, Kent Wallner, et al.
Clinical Genetics|February 28, 2004
Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like featuresC Pescucci, I Meloni, M Bruttini, et al.
Human Mutation|July 9, 2004
Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplicationFrancesca Ariani, Francesca Mari, Chiara Pescucci, et al.
Dose-Response : a Publication of International Hormesis Society|April 22, 2020
Replacing LNT: The Integrated LNT-Hormesis ModelCara Y Kaminski, Michael Dattoli, Joseph M Kaminski
Physical Review Letters|October 1, 2016
Compton Scattered X-Gamma Rays with Orbital MomentumV Petrillo, G Dattoli, I Drebot, et al.
Plos Genetics|May 20, 2021
CENP-C functions in centromere assembly, the maintenance of CENP-A asymmetry and epigenetic age in Drosophila germline stem cellsBen L Carty, Anna A Dattoli, Elaine M Dunleavy
Journal of Human Genetics|January 20, 2007
Frequency of the LRRK2 G2019S mutation in Italian patients affected by Parkinson's diseaseTiziana Squillaro, Franca Cambi, Giuseppe Ciacci, et al.
American Journal of Human Genetics|September 14, 2000
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in malesI Meloni, M Bruttini, I Longo, et al.
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